Ludwigsen S - Search Results

1

Integrated human genome-wide maps constructed using the CEPH reference panel.

Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Duyk GM, Sheffield VC, Wang Z, Murray JC. Buetow KH, et al. Among authors: ludwigsen s. Nat Genet. 1994 Apr;6(4):391-3. doi: 10.1038/ng0494-391. Nat Genet. 1994. PMID: 8054980

2

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).

Murray JC, Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Manion F, Quillen J, Sheffield VC, Sunden S, Duyk GM, et al. Murray JC, et al. Among authors: ludwigsen s. Science. 1994 Sep 30;265(5181):2049-54. doi: 10.1126/science.8091227. Science. 1994. PMID: 8091227

3

Human genetic map. Genome maps V. Wall chart.

Buetow KH, Ludwigsen S, Scherpbier-Heddema T, Quillen J, Murray JC, Sheffield VC, Duyk GM, Weber JL, Weissenbach J, Gyapay G, et al. Buetow KH, et al. Among authors: ludwigsen s. Science. 1994 Sep 30;265(5181):2055-70. doi: 10.1126/science.8091228. Science. 1994. PMID: 8091228 No abstract available.

4

A microsatellite-based multipoint index map of human chromosome 22.

Buetow KH, Duggan D, Yang B, Ludwigsen S, Puck J, Porter J, Budarf M, Spielman R, Emanuel BS. Buetow KH, et al. Among authors: ludwigsen s. Genomics. 1993 Nov;18(2):329-39. doi: 10.1006/geno.1993.1473. Genomics. 1993. PMID: 8288236

5

IsoSearch: An Untargeted and Unbiased Metabolite and Lipid Isotopomer Tracing Strategy from HR-LC-MS/MS Datasets.

Huang H, Yuan M, Seitzer P, Ludwigsen S, Asara JM. Huang H, et al. Among authors: ludwigsen s. Methods Protoc. 2020 Jul 30;3(3):54. doi: 10.3390/mps3030054. Methods Protoc. 2020. PMID: 32751454 Free PMC article.

6

Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.

Hershberger RE, Pinto JR, Parks SB, Kushner JD, Li D, Ludwigsen S, Cowan J, Morales A, Parvatiyar MS, Potter JD. Hershberger RE, et al. Among authors: ludwigsen s. Circ Cardiovasc Genet. 2009 Aug;2(4):306-13. doi: 10.1161/CIRCGENETICS.108.846733. Epub 2009 May 15. Circ Cardiovasc Genet. 2009. PMID: 20031601 Free PMC article.

7

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.

Hershberger RE, Parks SB, Kushner JD, Li D, Ludwigsen S, Jakobs P, Nauman D, Burgess D, Partain J, Litt M. Hershberger RE, et al. Among authors: ludwigsen s. Clin Transl Sci. 2008 May;1(1):21-6. doi: 10.1111/j.1752-8062.2008.00017.x. Clin Transl Sci. 2008. PMID: 19412328 Free PMC article.

8

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.

Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Peterson A, Li D, Jakobs P, Litt M, Porter CB, Rahko PS, Hershberger RE. Parks SB, et al. Among authors: ludwigsen s. Am Heart J. 2008 Jul;156(1):161-9. doi: 10.1016/j.ahj.2008.01.026. Epub 2008 Mar 12. Am Heart J. 2008. PMID: 18585512 Free PMC article.

9

Mutations of presenilin genes in dilated cardiomyopathy and heart failure.

Li D, Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Partain J, Nixon RR, Allen CN, Irwin RP, Jakobs PM, Litt M, Hershberger RE. Li D, et al. Among authors: ludwigsen s. Am J Hum Genet. 2006 Dec;79(6):1030-9. doi: 10.1086/509900. Epub 2006 Oct 24. Am J Hum Genet. 2006. PMID: 17186461 Free PMC article.

10

Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.

Kushner JD, Nauman D, Burgess D, Ludwigsen S, Parks SB, Pantely G, Burkett E, Hershberger RE. Kushner JD, et al. Among authors: ludwigsen s. J Card Fail. 2006 Aug;12(6):422-9. doi: 10.1016/j.cardfail.2006.03.009. J Card Fail. 2006. PMID: 16911908

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